Sklar Instruments recalls medical procedure kits with potential sterile barrier breaches. Affected kits have specific model numbers and lot codes. Consumers should check their kits for packaging issues.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments is recalling medical procedure kits that may have packaging issues leading to breaches in the sterile barrier. This could allow contamination during surgery, posing a risk of infection to patients.
The packaging may breach, allowing non-sterile materials to enter the kit. This could lead to contamination during eye surgery, increasing infection risk for patients.
Medical professionals and patients who use these kits for eye surgery procedures. Those with the specific model numbers and lot codes listed are most at risk.
Check for model numbers 96-2540, 96-2541, 96-2542, or 96-2542M with specific lot codes (FSS10 or MSS10). These kits are labeled for eye surgery procedures.
Look for model numbers and lot codes listed in the recall notice to determine if your kit is affected.
The recall states there are reports of packaging issues that may breach the sterile barrier, so they are not safe to use without checking the recall.
The recall does not specify a remedy, so you should check the kit's model and lot codes and contact Sklar Instruments for further instructions.
Check for model numbers 96-2540, 96-2541, 96-2542, or 96-2542M with lot codes FSS10 or MSS10.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0950-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0950-2025 from Sklar Instruments. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.